Canonical Allele Identifier: CA2771464173
Gene: EYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63984639_63984642del , CM000668.2:g.63984639_63984642del GRCh38
NC_000006.11:g.64694532_64694535del , CM000668.1:g.64694532_64694535del GRCh37
NC_000006.10:g.64752491_64752494del NCBI36
NG_023443.1:g.1727585_1727588del
NG_023443.2:g.1727585_1727588del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6835-38_6835-35del MANE Select ENSP00000424243.1:n.6835-38_6835-35del
ENST00000370616.6:c.6835-38_6835-35del ENSP00000359650.2:n.6835-38_6835-35del
ENST00000370618.7:c.6835-38_6835-35del ENSP00000359652.4:n.6835-38_6835-35del
ENST00000370621.7:c.6835-38_6835-35del ENSP00000359655.3:n.6835-38_6835-35del
ENST00000398580.3:c.149-38_149-35del
ENST00000503581.5:c.6835-38_6835-35del ENSP00000424243.1:n.6835-38_6835-35del
NM_001142800.1:c.6835-38_6835-35del NP_001136272.1:n.6835-38_6835-35del
NM_001292009.1:c.6835-38_6835-35del NP_001278938.1:n.6835-38_6835-35del
XR_001744188.1:n.606+16355_606+16358del
XR_001744189.1:n.129+16355_129+16358del
XR_001744190.1:n.197+16355_197+16358del
XR_001744191.1:n.607-1015_607-1012del
NM_001142800.2:c.6835-38_6835-35del MANE Select NP_001136272.1:n.6835-38_6835-35del
NM_001292009.2:c.6835-38_6835-35del NP_001278938.1:n.6835-38_6835-35del